NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Effect of carryover of clot activators on coagulation tests during phlebotomy.

Author(s): Fukugawa Y, Ohnishi H, Ishii T, Tanouchi A, Sano J, Miyawaki H, Kishino T, Ohtsuka K, Yoshino H, Watanabe T

Publication: Am J Clin Pathol, 2012, Vol. 137, Page 900-3

PubMed ID: 22586048 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of clot activators on coagulation testing.

Conclusion of Paper

The addition of clot activators in vitro to specimens intended for coagulation testing resulted in minimal but significant changes in prothrombin time (PT) and activated partial thromboplastin time (aPTT). On the other hand, fibrin monomer complex (FMC) was significantly and remarkably affected by the addition of clot activator fluid containing thrombin. In specimens from healthy individuals and patients on warfarin, PT was minimally but significantly affected by tube draw order when coagulation tubes were drawn before and after serum tubes containing clot activator. Fibrinogen was also affected by tube draw order, but only for specimens from patients on warfarin. Other coagulation parameters were not affected by tube draw order.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of the addition of clot activator fluid to blood specimens in vitro on PT, aPTT, fibrinogen, D-dimer, and FMC measurements. Specimens were collected in sodium citrate Venoject II tubes, and clot activator fluid was added which had been prepared by adding saline to Venoject II tubes containing either thrombin and glass particles or only glass particles, or by adding saline to Vacutainer tubes containing silica particles. Coagulation testing was performed immediately after centrifugation.

    Summary of Findings:

    PT was significantly increased by the addition of any amount of clot activator fluid containing thrombin, glass particles, or silica particles, but all values were within 3% of the controls (saline added). aPTT was significantly decreased and FMC was significantly increased by the addition of thrombin clot activator fluid, and the changes were proportional to the amount of fluid added. The effects of glass and silica particle clot activator fluid on aPTT and FMC were minimal. Fibrinogen and D-dimer were generally not affected by the addition of any clot activator fluid, although some random significant changes were observed.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Morphology Hematology/ auto analyzer
    Glycoprotein Hematology/ auto analyzer
    Peptide Hematology/ auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Aliquots and Components Biospecimen components 2 uL clot activator fluid
    5 uL clot activator fluid
    10 uL clot activator fluid
    2 uL saline
    5 uL saline
    10 uL saline
    Thrombin and glass particles
    Glass particles
    Silica particles
  2. Study Purpose

    The purpose of this study was to determine the effects of draw order when using a serum tube containing thrombin and glass particles and a coagulation tube containing sodium citrate on PT, aPTT, fibrinogen, D-dimer, and FMC measurements. Blood specimens were collected in the following order: plain tube with no additives, coagulation tube with sodium citrate, serum tube with thrombin and glass particles, and another coagulation tube. The butterfly needle inside the serum tube was purposefully soaked in the blood specimen during draw to maximize the possibility of clot activator contamination in the last coagulation tube.

    Summary of Findings:

    Among specimens from healthy volunteers and patients on warfarin, the average PT ratio and international normalized ration (INR) were lower in the coagulation tube drawn after the serum tube containing clot activator than in the coagulation tube drawn before the serum tube. For specimens from patients on warfarin, fibrinogen was significantly higher in the coagulation tube drawn after the serum tube compared to the one drawn before. No other differences in coagulation tests were noted between the two coagulation tubes for healthy volunteers or patients on warfarin.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Normal
    • Cardiovascular Disease
    Platform:
    AnalyteTechnology Platform
    Morphology Hematology/ auto analyzer
    Glycoprotein Hematology/ auto analyzer
    Peptide Hematology/ auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Preaquisition Other drugs Warfarin
    None
    Biospecimen Acquisition Type of collection container/solution Plain tube
    Coagulation tube with sodium citrate
    Serum tube with thrombin and glass particles
    Biospecimen Aliquots and Components Aliquot sequential collection Plasma tube filled after plain tube
    Plasma tube filled after serum tube containing clot activator

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